RecallRadar

FDA Drug recall D-0204-2017

Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL (20 mg/mL) ,Single-Dose Syringe Injection Solution, For Slow IV Use Only ,Rx…

On 2016-12-21 the FDA classified a Class II recall of Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL (20 mg/mL) ,Single-Dose Syringe Injection Solution, For Slow IV Use Only ,Rx… by Cantrell Drug, citing lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0204-2017
ClassificationClass II
Statusterminated
Initiated2016-11-18
Published2016-12-21
Last updated2026-09-13 11:51 UTC
CompanyCantrell Drug
DistributionUS

Product

Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL (20 mg/mL) ,Single-Dose Syringe Injection Solution, For Slow IV Use Only ,Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-067-12

Reason

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Identifiers

code_infoLot: 169262 BUD: 1/8/2017, Lot: 169812 BUD: 1/19/2017

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0204-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.